Structure of PDB 3ejd Chain H Binding Site BS02
Receptor Information
>3ejd Chain H (length=382) Species:
1423
(Bacillus subtilis) [
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ASSEFLKNPYSFYDTLRAVHPIYKGSFLKYPGWYVTGYEETAAILKDARF
KVRTPLPESSTKYQDLSHVQNQMMLFQNQPDHRRLRTLASGAFTPRTTES
YQPYIIETVHHLLDQVQGKKKMEVISDFAFPLASFVIANIIGVPEEDREQ
LKEWAASLIQTIDFTRSRKALTEGNIMAVQAMAYFKELIQKRKRHPQQDM
ISMLLKGDKLTEEEAASTCILLAIAGHETTVNLISNSVLCLLQHPEQLLK
LRENPDLIGTAVEECLRYESPTQMTARVASEDIDICGVTIRQGEQVYLLL
GAANRDPSIFTNPDVFDITRSPNPHLSFGHGHHVCLGSSLARLEAQIAIN
TLLQRMPSLNLADWRYRPLFGFRALEELPVTF
Ligand information
Ligand ID
HEM
InChI
InChI=1S/C34H34N4O4.Fe/c1-7-21-17(3)25-13-26-19(5)23(9-11-33(39)40)31(37-26)16-32-24(10-12-34(41)42)20(6)28(38-32)15-30-22(8-2)18(4)27(36-30)14-29(21)35-25;/h7-8,13-16H,1-2,9-12H2,3-6H3,(H4,35,36,37,38,39,40,41,42);/q;+2/p-2/b25-13-,26-13-,27-14-,28-15-,29-14-,30-15-,31-16-,32-16-;
InChIKey
KABFMIBPWCXCRK-RGGAHWMASA-L
SMILES
Software
SMILES
OpenEye OEToolkits 1.7.6
Cc1c2n3c(c1CCC(=O)O)C=C4C(=C(C5=[N]4[Fe]36[N]7=C(C=C8N6C(=C5)C(=C8C)C=C)C(=C(C7=C2)C)C=C)C)CCC(=O)O
CACTVS 3.385
CC1=C(CCC(O)=O)C2=Cc3n4[Fe]5|6|N2=C1C=c7n5c(=CC8=N|6C(=Cc4c(C)c3CCC(O)=O)C(=C8C=C)C)c(C)c7C=C
ACDLabs 12.01
C=1c3c(c(c4C=C5C(=C(C=6C=C7C(=C(C8=CC=2C(=C(C=1N=2[Fe](n34)(N5=6)N78)CCC(=O)O)C)\C=C)C)\C=C)C)C)CCC(=O)O
Formula
C34 H32 Fe N4 O4
Name
PROTOPORPHYRIN IX CONTAINING FE;
HEME
ChEMBL
DrugBank
DB18267
ZINC
PDB chain
3ejd Chain H Residue 405 [
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Receptor-Ligand Complex Structure
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PDB
3ejd
Structural insights from a P450 Carrier Protein complex reveal how specificity is achieved in the P450(BioI) ACP complex.
Resolution
2.1 Å
Binding residue
(original residue number in PDB)
M80 L81 H88 R92 A234 T238 T239 P280 T284 R286 S336 F337 H342 C344 L345 G346 L349 A350
Binding residue
(residue number reindexed from 1)
M74 L75 H82 R86 A225 T229 T230 P271 T275 R277 S327 F328 H333 C335 L336 G337 L340 A341
Annotation score
1
Enzymatic activity
Catalytic site (original residue number in PDB)
Q166 A234 E237 T238 T239 C344 L345 G346 E353 F383
Catalytic site (residue number reindexed from 1)
Q160 A225 E228 T229 T230 C335 L336 G337 E344 F372
Enzyme Commision number
1.14.14.46
: pimeloyl-[acyl-carrier protein] synthase.
Gene Ontology
Molecular Function
GO:0004497
monooxygenase activity
GO:0005506
iron ion binding
GO:0016705
oxidoreductase activity, acting on paired donors, with incorporation or reduction of molecular oxygen
GO:0020037
heme binding
GO:0046872
metal ion binding
Biological Process
GO:0009102
biotin biosynthetic process
View graph for
Molecular Function
View graph for
Biological Process
External links
PDB
RCSB:3ejd
,
PDBe:3ejd
,
PDBj:3ejd
PDBsum
3ejd
PubMed
18838690
UniProt
P53554
|BIOI_BACSU Biotin biosynthesis cytochrome P450 (Gene Name=bioI)
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